Human Amniotic Epithelial Stem Cells Alleviate Autoimmune Premature Ovarian Insufficiency in Mice by Targeting Granulosa Cells via AKT/ERK Pathways.

IF 4.5 3区 医学 Q2 CELL & TISSUE ENGINEERING Stem Cell Reviews and Reports Pub Date : 2024-08-01 Epub Date: 2024-06-04 DOI:10.1007/s12015-024-10745-z
Xiaohang Ye, Yifeng Lin, Yanyun Ying, Xuezhi Shen, Feida Ni, Feixia Wang, Jianpeng Chen, Wei Zhao, Xiaoming Yu, Dan Zhang, Yifeng Liu
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Abstract

Autoimmune factors play an important role in premature ovarian insufficiency (POI). Human amniotic epithelial stem cells (hAESCs) have recently shown promising treatment effects on chemotherapy-induced POI. However, the therapeutic efficacy and underlying mechanisms of hAESCs in autoimmune POI remain to be investigated. In this study, we showed for the first time that intravenous transplantation of hAESCs could reside in the ovary of zona pellucida 3 peptide (pZP3) induced autoimmune POI mice model for at least 4 weeks. hAESCs could improve ovarian function and fertility, alleviate inflammation and reduce apoptosis of granulosa cells (GCs) in autoimmune POI mice. The transcriptome analysis of mice ovaries and in vitro co-cultivation experiments suggest that activation of the AKT and ERK pathways may be the key mechanism in the therapeutic effect of hAESCs. Our work provides the theoretical and experimental foundation for optimizing the administration of hAESCs, as well as the clinical application of hAESCs in autoimmune POI patients.

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人羊膜上皮干细胞通过 AKT/ERK 通路靶向颗粒细胞缓解小鼠自身免疫性早发性卵巢发育不全症
自身免疫因素在卵巢早衰(POI)中扮演着重要角色。最近,人羊膜上皮干细胞(hAESCs)对化疗引起的早发性卵巢功能不全显示出了良好的治疗效果。然而,hAESCs对自身免疫性POI的疗效和内在机制仍有待研究。在这项研究中,我们首次发现静脉移植hAESCs可在透明带3肽(pZP3)诱导的自身免疫性POI小鼠模型的卵巢中存活至少4周。hAESCs可改善自身免疫性POI小鼠的卵巢功能和生育能力,缓解炎症并减少颗粒细胞(GCs)的凋亡。小鼠卵巢转录组分析和体外联合培养实验表明,激活AKT和ERK通路可能是hAESCs治疗效果的关键机制。我们的研究为优化hAESCs的用药以及hAESCs在自身免疫性卵巢炎患者中的临床应用提供了理论和实验基础。
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来源期刊
Stem Cell Reviews and Reports
Stem Cell Reviews and Reports 医学-细胞生物学
CiteScore
9.30
自引率
4.20%
发文量
0
审稿时长
3 months
期刊介绍: The purpose of Stem Cell Reviews and Reports is to cover contemporary and emerging areas in stem cell research and regenerative medicine. The journal will consider for publication: i) solicited or unsolicited reviews of topical areas of stem cell biology that highlight, critique and synthesize recent important findings in the field. ii) full length and short reports presenting original experimental work. iii) translational stem cell studies describing results of clinical trials using stem cells as therapeutics. iv) papers focused on diseases of stem cells. v) hypothesis and commentary articles as opinion-based pieces in which authors can propose a new theory, interpretation of a controversial area in stem cell biology, or a stem cell biology question or paradigm. These articles contain more speculation than reviews, but they should be based on solid rationale. vi) protocols as peer-reviewed procedures that provide step-by-step descriptions, outlined in sufficient detail, so that both experts and novices can apply them to their own research. vii) letters to the editor and correspondence. In order to facilitate this exchange of scientific information and exciting novel ideas, the journal has created five thematic sections, focusing on: i) the role of adult stem cells in tissue regeneration; ii) progress in research on induced pluripotent stem cells, embryonic stem cells and mechanism governing embryogenesis and tissue development; iii) the role of microenvironment and extracellular microvesicles in directing the fate of stem cells; iv) mechanisms of stem cell trafficking, stem cell mobilization and homing with special emphasis on hematopoiesis; v) the role of stem cells in aging processes and cancerogenesis.
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